Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
interleukin 1 receptor accessory protein like 1
Summary
- Gene Symbol
-
- IL1RAPL1
- Aliases
-
- IL1R8
- OPHN4
- TIGIRR-2
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Cell membrane
- Cell projection
- Cytoplasm
- Disulfide bond
- Glycoprotein
- Hydrolase
- Immunoglobulin domain
- Intellectual disability
- NAD
- Receptor
- Reference proteome
- Repeat
- Signal
- Transmembrane helix
- Proteins
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| heterophilic cell-cell adhesion via plasma membrane cell adhesion molecules |
|
|
| positive regulation of dendritic spine morphogenesis | ||
| negative regulation of exocytosis | ||
| positive regulation of synapse assembly | ||
| neuron differentiation |
GO Hierarchy
biological process
biological regulation [inference]
regulation of biological process [inference]
positive regulation of biological process [inference]
regulation of developmental process [inference]
regulation of cellular process [inference]
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| NAD+ nucleosidase activity | ||
| NAD+ nucleotidase, cyclic ADP-ribose generating | ||
| signaling receptor binding | ||
| interleukin-1 binding | ||
| protein binding |
GO Hierarchy
Rhea
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0050745 | diffuse large B-cell lymphoma | |
| DOID:0050776 | non-syndromic X-linked intellectual disability | |
| DOID:0060041 | autism spectrum disorder | |
| DOID:0060427 | chromosome Xp21 deletion syndrome | |
| DOID:0060823 | syndromic X-linked intellectual disability 94 | |
| DOID:0080156 | X-linked adrenal hypoplasia congenita | |
| DOID:0112022 | non-syndromic X-linked intellectual disability 21 | |
| DOID:1059 | intellectual disability | |
| DOID:1094 | attention deficit hyperactivity disorder | |
| DOID:114 | heart disease |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000053 | Macroorchidism |
| HP:0000194 | Open mouth |
| HP:0000303 | Mandibular prognathia |
| HP:0000316 | Hypertelorism |
| HP:0000486 | Strabismus |
| HP:0000582 | Upslanted palpebral fissure |
| HP:0000664 | Synophrys |
| HP:0000678 | Dental crowding |
| HP:0000717 | Autism |
| HP:0000752 | Hyperactivity |
| Disease ID | Disease Name |
|---|---|
| OMIM:300143 |
|
PubChem Disease
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 118313039 | SCOMX15063 | ||
| 117030144 | RHIFE17524 | ||
| 101817250 | FICAL09826 | ||
| 100604188 | NOMLE38290 | ||
| 114596199 | PODMU19929 | ||
| 105304717 | PTEVA15671 | ||
| 115055063 | ECHNA17744 | ||
| 105814723 | PROCO24747 | ||
| 109084617 | CYPCA120792 | ||
| 109112414 | CYPCA125070 |
